首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and spectral determination of new derivatives of 1-[(p-substituted)phenyl]-3a-[(o- and p-substituted)phenyl]-5-chloro-9-methylthio-10,3a-dihydro-[1,2,4]-oxadiazolo[2,3-b][1,4]benzodiazepines
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Synthesis and spectral determination of new derivatives of 1-[(p-substituted)phenyl]-3a-[(o- and p-substituted)phenyl]-5-chloro-9-methylthio-10,3a-dihydro-[1,2,4]-oxadiazolo[2,3-b][1,4]benzodiazepines

机译:1-[(对位取代)苯基] -3a-[(对位和对位取代)苯基] -5-氯-9-甲硫基-10,3a-二氢-[1,1]的新衍生物的合成和光谱测定2,4]-恶二唑[2,3-b] [1,4]苯并二氮杂

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摘要

A new synthesis to obtain eight novel derivatives of 1-[(p-substituted)phenyl]-3a-[(o- and p-substituted)phenyl]-5-chloi-o-9-methylthio-10,3a-dihydro-[1,2,4]-oxadiazolo[2,3-b][1,4]benzodiazepines with possible biological and pharmacological activity as anxiolytics, hypnotics, anticonvulsants in the central nervous system. The final products were obtained by condensation between 2-methylthio-5-[(o-; p-substituted)phenyl]-3H-7-chloro-[1,4]benzodiazepine with benzonitrile oxide generated in situ from benzohydroxamoyl chloride in triethylamine. The structure of all products was corroborated by ir, H-1-nmr, C-13-nmr, with experiments bidimensional and ms in low and high resolution.
机译:一种新的合成方法,可获得八个[1-[(对位取代的)苯基] -3a-[(对位和对位取代的)苯基] -5-氯-o-9-甲硫基-10,3a-二氢- [1,2,4]-恶二唑并[2,3-b] [1,4]苯并二氮杂with在中枢神经系统中可能具有抗焦虑药,催眠药和抗惊厥药的生物学和药理活性。通过使2-甲硫基-5-[(邻-,对-取代的)苯基] -3H-7-氯代-[1,4]苯并二氮杂卓与苯甲腈在三乙胺中原位生成的苄腈氧化物缩合而获得最终产物。 ir,H-1-nmr,C-13-nmr证实了所有产品的结构,并在低分辨率和高分辨率下进行了二维和ms实验。

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